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Global electrical heterogeneity phenotypes

TBX3 · rs7301677

What the study found

Who was studied 3,057 Black individuals, 10,769 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.14 higher (95% confidence interval 0.11-0.17); p = 2 × 10−24.

How common The T allele had a frequency of about 26% in the people studied.

Where it sits Chromosome 12, band 12q24.21 — between genes, 4.8 kb from LOC124903080.

What each result means

C/C No copy of the version the research linked to Global electrical heterogeneity phenotypes. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Global electrical heterogeneity phenotypes. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Global electrical heterogeneity phenotypes. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs7301677

What is rs7301677?

rs7301677 is a single position in the genome, in or near the TBX3 gene. Published research associates it with global electrical heterogeneity phenotypes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7301677 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs7301677 come from?

GWAS Catalog, J Am Heart Assoc 2018, PMID:29622589. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Global electrical heterogeneity phenotypes (rs7301677). MyGeneLog™. https://www.mygenelog.com/variants/rs7301677

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